Antimalarial & Antiprotozoal

Sodium StibogluconateThird Party Manufacturing in India

Looking to get Sodium Stibogluconate manufactured under your brand? Our WHO-GMP certified partner facilities support PCD franchise partners and global export opportunities structured across 25+ countries.

WHO-GMP Certified
Export Ready
PCD Franchise Available
CAS Number
16037-91-5
Drug Class
Pentavalent antimonial (Antileishmanial)
Molecular Formula
C₁₂H₁₆O₁₇Sb₂·3Na·9H₂O
Molecular Weight
907.88 g/mol
Grade Standards
IP, BP, USP
Therapeutic Category
Antimalarial & Antiprotozoal
MOQ
Contact us for MOQ — varies by formulation and packaging
Dosage Forms
Injection

Mechanism of Action

Sodium Stibogluconate works as a pentavalent antimonial compound that exerts its antileishmanial effect through multiple mechanisms. It is thought to act as a prodrug that is converted intracellularly to the more active trivalent antimony form within the Leishmania parasite and in the acidic compartments of macrophages.

The active trivalent antimony binds to sulfhydryl-containing biomolecules including trypanothione, a key thiol in Leishmania parasites, disrupting the parasite's antioxidant defense system. It also inhibits parasitic type I DNA topoisomerase, interfering with DNA replication and repair. Additionally, Sodium Stibogluconate modulates the host immune response by inhibiting protein tyrosine phosphatases such as SHP-1 and SHP-2, leading to enhanced cytokine signaling and macrophage activation.

Unlike many other antiprotozoal agents, Sodium Stibogluconate combines direct parasiticidal activity with host immune modulation. It is highly effective against visceral leishmaniasis, cutaneous leishmaniasis, and mucocutaneous leishmaniasis, and remains a WHO-recommended first-line treatment in many endemic regions.

Therapeutic Uses & Indications

Therapeutic Uses

Sodium Stibogluconate is prescribed for the treatment of:

  • Visceral Leishmaniasis (Kala-azar): First-line treatment for systemic Leishmania donovani infection affecting the spleen, liver, and bone marrow.
  • Cutaneous Leishmaniasis: Treatment of skin ulcers caused by Leishmania species, including Leishmania tropica and Leishmania major.
  • Mucocutaneous Leishmaniasis: Management of destructive lesions of the nasopharyngeal mucosa caused by Leishmania braziliensis complex.
  • Post-Kala-azar Dermal Leishmaniasis: Treatment of skin manifestations that can follow visceral leishmaniasis.

Why Manufacturers Choose Sodium Stibogluconate

Leishmaniasis remains a significant public health problem in tropical and subtropical regions, with millions at risk worldwide. Sodium Stibogluconate, marketed historically as Pentostam, has been in continuous clinical use for over half a century and is included in the WHO Essential Medicines List. Despite newer therapies, it remains indispensable for endemic regions in the Indian subcontinent, East Africa, and Latin America.

This makes Sodium Stibogluconate an essential antiprotozoal for third party manufacturing in India, serving WHO treatment programs and export to endemic countries with ongoing disease burden.

Dosage Forms We Manufacture

Injection
100mg/ml (SbV) · 330mg/ml (SbV)

Frequently Asked Questions

What is the minimum order quantity for Sodium Stibogluconate?
Minimum order quantity for Sodium Stibogluconate is Contact us for MOQ — varies by formulation and packaging. Please contact us for bulk pricing and custom quantities.
What dosage forms of Sodium Stibogluconate can you manufacture?
We manufacture Sodium Stibogluconate as: Injection (100mg/ml (SbV), 330mg/ml (SbV)).
Are your manufacturing facilities WHO-GMP certified?
Yes. Celesta Healthcare works exclusively with WHO-GMP certified partner production facilities. All manufacturing batches are subject to strict quality control and documentation.
Can you manufacture Sodium Stibogluconate for export?
Yes. We provide export-ready Sodium Stibogluconate formulations structured across 25+ countries. We provide full export documentation including Certificate of Analysis (CoA), Certificate of Origin, and regulatory dossiers on request.
What grade standards do you follow for Sodium Stibogluconate?
We manufacture Sodium Stibogluconate to IP, BP, USP pharmacopoeial standards.
Third Party Manufacturing

Get Sodium Stibogluconate made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • Low MOQ, export ready
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Our Manufacturing Capabilities

  • WHO-GMP Certified Partner Plants
  • 25+ years of pharma industry experience
  • PCD Franchise with monopoly rights
  • Export support across 25+ countries
  • Small batch to commercial scale
  • Custom formulation development

Packaging Options

Glass vials or ampoules in mono cartons. Packaging customized to client brand guidelines.

Start Manufacturing Sodium Stibogluconate Today

Celesta Healthcare provides WHO-GMP certified third-party manufacturing for Sodium Stibogluconate across all dosage forms. PCD franchise and export orders welcome.

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